5-MeO-DMT
Data klinis
Rute
pemberian		Dihisap, Dihirup, Oral
Status hukum
Status hukum
Pengenal
  • 2-(5-Metoksi-1H-indol-3-il)-N,N-dimetiletanamina
Nomor CAS
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.012.558 Sunting di Wikidata
Data sifat kimia dan fisik
RumusC13H18N2O
Massa molar218,30 g·mol−1
Model 3D (JSmol)
  • COc2ccc1[nH]cc(CCN(C)C)c1c2
  • InChI=1S/C13H18N2O/c1-15(2)7-6-10-9-14-13-5-4-11(16-3)8-12(10)13/h4-5,8-9,14H,6-7H2,1-3H3 checkY
  • Key:ZSTKHSQDNIGFLM-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

5-MeO-DMT (5-metoksi-N,N-dimetiltriptamina) atau O-metil-bufotenin adalah obat psikedelik dari golongan triptamin. Zat ini ditemukan dalam berbagai spesies tanaman, dan disekresikan oleh kelenjar dari setidaknya satu spesies katak, yaitu katak sungai colorado. Seperti kerabat dekatnya, DMT dan bufotenin (5-HO-DMT), senyawa ini telah digunakan sebagai enteogen di Amerika Selatan.[1] 5-MeO-DMT sering dirujuk dengan beberapa slang seperti Five-methoxy, The power, dan Toad venom.[2]

Referensi

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  1. ^ Araújo AM, Carvalho F, Bastos M, Guedes de Pinho P, Carvalho M (August 2015). "The hallucinogenic world of tryptamines: an updated review". Archives of Toxicology. 89 (8): 1151–73. doi:10.1007/s00204-015-1513-x. PMID 25877327. S2CID 4825078.
  2. ^ "Ultimate Guide to 5-MeO-DMT - Experience, Benefits, & Side Effects". 29 June 2020.

Pranala luar

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📚 Artikel Terkait di Wikipedia

Kemuning

paniculatin, tannin, dan coumurrayin. Kulit batang mengandung mexotioin, 5-7-dimethoxy-8 (2,3-dihydroxyisopentyl) coumarin. Sedangkan bunga kemuning mengandung

Kaki seribu

PMID 12216861. S2CID 30068731. Wood, William F. (1974). "Toluquinone and 2-Methoxy-3-methylbenzoquinone from the Defensive Secretions of Three African Millipedes"

Bedakuilin

eliminasi 5,5 bulan Ekskresi Feses Pengenal Nama IUPAC (1R,2S)-1-(6-Bromo-2-methoxy-3-quinolyl)-4-dimethylamino-2-(1-naphthyl)-1-phenylbutan-2-ol Nomor CAS

Miristisin

1996). "Analysis of 1-(3-Methoxy-4,5-Methylenedioxyphenyl)-2-Propanamine (MMDA) Derivatives Synthesized from Nutmeg Oil and 3-Methoxy-4,5-Methylenedioxybenzaldehyde"

Polistirena sulfonat

1002/14356007.a14_393.pub2. ISBN 978-3527306732. (2009) "Stereoselective Synthesis of anti α-Methyl-β-Methoxy Carboxylic Compounds". Org. Synth. 86: 81. 

Triptamina

(2012). "Head-twitch response in rodents induced by the hallucinogen 2,5-dimethoxy-4-iodoamphetamine: a comprehensive history, a re-evaluation of mechanisms

Fensiklidina

Roth BL, dkk (2013). "The ketamine analogue methoxetamine and 3- and 4-methoxy analogues of phencyclidine are high affinity and selective ligands for

Borat

(link) R. L. Kidwell, M. Murphy, and S. D. Darling (1969). "Phenols: 6-Methoxy-2-naphthol". Org. Synth. 49: 90; Coll. Vol. 10: 80.  Wikimedia Commons